L-TGA is just one of many congenital heart defects..but yet a very rare one, making it harder to find information about..I hope this group will help give support,finding information on this chd and different medical options that are availble for thid chd.
My name is Marty and my son Bradley was born August 2,1999 with L-TGA..he also had coarctaion of the aorta repaired at 3 days old..he developed Bradycardia and a pacemaker was implanted when he was 3 months old his left av valve has been leaking since he was 2 months old,they continue to keep a watch on it..
We would like to invite you to share your stories and exsperiences.We look foward to meeting you.